(Q52270154)

English

Supernumerary microchromosomes identified as inverted duplications of chromosome 15: a report of three cases.

scientific article published in January 1985

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

28 April 2018

http://europepmc.org/abstract/MED/3972417

Supernumerary microchromosomes identified as inverted duplications of chromosome 15: a report of three cases. (English)

1 reference

Europe PubMed Central

PubMed publication ID

28 April 2018

http://europepmc.org/abstract/MED/3972417

author name string

L P Wisniewski

1

1 reference

Europe PubMed Central

PubMed publication ID

28 April 2018

http://europepmc.org/abstract/MED/3972417

R A Doherty

2

1 reference

Europe PubMed Central

PubMed publication ID

28 April 2018

http://europepmc.org/abstract/MED/3972417

publication date

1 January 1985

1 reference

Europe PubMed Central

PubMed publication ID

28 April 2018

http://europepmc.org/abstract/MED/3972417

1 reference

Europe PubMed Central

PubMed publication ID

28 April 2018

http://europepmc.org/abstract/MED/3972417

69

1 reference

Europe PubMed Central

PubMed publication ID

28 April 2018

http://europepmc.org/abstract/MED/3972417

2

1 reference

Europe PubMed Central

PubMed publication ID

28 April 2018

http://europepmc.org/abstract/MED/3972417

161-163

1 reference

Europe PubMed Central

PubMed publication ID

28 April 2018

http://europepmc.org/abstract/MED/3972417

https://scigraph.springernature.com/pub.10.1007/bf00293289

0 references

Supernumerary chromosomes in six patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/3972417

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An extra idic(15p)(q11) chromosome in Prader-Willi syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/3972417

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytogenetic and clinical studies in five cases of inv dup(15)

1 reference

https://pubmed.ncbi.nlm.nih.gov/3972417

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prader-Willi syndrome and a bisatellited derivative of chromosome 15

1 reference

https://pubmed.ncbi.nlm.nih.gov/3972417

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Accessory small chromosomes in amniotic fluid cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/3972417

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Preferential maternal derivation in inv dup(15): analysis of eight new cases.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3972417

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome 15 abnormalities and the Prader-Willi syndrome: a follow-up report of 40 cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/3972417

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Partial trisomy 15 in a male with severe psychomotor retardation (48, XY, + 15q -, + mar(15))

1 reference

https://pubmed.ncbi.nlm.nih.gov/3972417

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Preferential derivation of abnormal human G-group-like chromosomes from chromosome 15

1 reference

https://pubmed.ncbi.nlm.nih.gov/3972417

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prader-Willi syndrome and chromosome 15. A clinical discussion of 20 cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/3972417

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal detection of an accessory chromosome identified as an inversion duplication (15)

1 reference

https://pubmed.ncbi.nlm.nih.gov/3972417

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00293289

1 reference

Europe PubMed Central

PubMed publication ID

28 April 2018

http://europepmc.org/abstract/MED/3972417

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 April 2018

http://europepmc.org/abstract/MED/3972417

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